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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050453 | lissencephaly | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:0112232 | lissencephaly 3 | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:0112234 | microlissencephaly | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:0080918 | polymicrogyria | HGNC:18809 | Homo sapiens (human) | 10376 | TUBA1B |
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| DOID:1184 | nephrotic syndrome | HGNC:18816 | Homo sapiens (human) | 84063 | KIRREL2 |
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| DOID:557 | kidney disease | HGNC:18816 | Homo sapiens (human) | 84063 | KIRREL2 |
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| DOID:9206 | Barrett's esophagus | HGNC:18831 | Homo sapiens (human) | 115908 | CTHRC1 |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:18838 | Homo sapiens (human) | 10848 | PPP1R13L |
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| DOID:0050737 | autosomal recessive disease | HGNC:18838 | Homo sapiens (human) | 10848 | PPP1R13L |
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| DOID:1324 | lung cancer | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:1485 | cystic fibrosis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:850 | lung disease | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:9351 | diabetes mellitus | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:13580 | cholestasis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:693 | dental enamel hypoplasia | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0060643 | primary sclerosing cholangitis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:13316 | exocrine pancreatic insufficiency | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:13166 | allergic bronchopulmonary aspergillosis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:9563 | bronchiectasis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:1793 | pancreatic cancer | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:5733 | salpingitis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0050127 | sinusitis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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